Exercise and training effects on ceramide metabolism in human skeletal muscle

被引:66
作者
Helge, JW
Dobrzyn, A
Saltin, B
Gorski, J
机构
[1] Univ Copenhagen, Natl Hosp, Muscle Res Ctr, Copenhagen, Denmark
[2] Med Univ Bialystok, Dept Physiol, Bialystok, Poland
关键词
D O I
10.1113/expphysiol.2003.002605
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In rat skeletal muscle prolonged exercise affects the content and composition of ceramides, but in human skeletal muscle no data are available on this compound. Our aim was to examine the content of ceramide- and sphingomyelin fatty acids and neutral, Mg2+-dependent sphingomyelinase activity in skeletal muscle in untrained and trained subjects before and after prolonged exercise. Healthy male subjects were recruited into an untrained (n = 8, Vo(2),max 3.8 +/- 0.2 l min(1)) and a trained (n = 8, Vo(2),max 5.1 +/- 0.1 l min(1)) group. Before and after a 3-h exercise bout (58 +/- 1% Vo(2),max) a muscle biopsy was excised from the vastus lateralis. Ceramide and sphingomyelin were isolated using thin-layer chromatography. The content of individual ceramide fatty acids and sphingomyelin fatty acids was measured by means of gas-liquid chromatography. The activity of neutral, Mg2+-dependent sphingomyelinase was measured using N-[(CH3)-C-14]-sphingomyelin as a substrate. Prior to exercise, the muscle total ceramide fatty acid content in both groups was similar (201 +/- 18 and 197 +/- 9 nmol g(-1) in the untrained and trained group, respectively) and after exercise a 25% increase in the content was observed in each group. At rest, the muscle total sphingomyelin fatty acid content was higher in untrained than in trained subjects (456 +/- 10, 407 +/- 7 nmol g(-1), respectively; P < 0.05). After exercise a 20% increase (P < 0.05) in total sphingomyelin was observed only in the trained subjects. The muscle neutral, Mg2+-dependent sphingomyelinase activity was similar in the two groups at rest and a similar reduction was observed after exercise in both groups (untrained from 2.19 +/- 0.08 to 1.78 +/- 0.08 and trained from 2.31 +/- 0.12 to 1.80 +/- 0.09 nmol (mg protein)(-1) h(-1); P < 0.05 in each case). In conclusion, we have reported, for the first time, the values for ceramide fatty acid content and neutral, Mg2+-dependent sphingomyelinase activity in human skeletal muscle. The results indicate that acute prolonged exercise affects ceramide metabolism in human skeletal muscle both in untrained and in trained subjects and this may influence muscle cell adaptation and metabolism.
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页码:119 / 127
页数:9
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共 31 条
  • [11] Modulation of cell signalling by ceramides
    Gómez-Muñoz, A
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1998, 1391 (01): : 92 - 109
  • [12] Görski J, 2002, ANN NY ACAD SCI, V967, P236
  • [13] MUSCLE GLYCOGEN DURING PROLONGED SEVERE EXERCISE
    HERMANSE.L
    HULTMAN, E
    SALTIN, B
    [J]. ACTA PHYSIOLOGICA SCANDINAVICA, 1967, 71 (2-3): : 129 - &
  • [14] Lipid-induced insulin resistance in human muscle is associated with changes in diacylglycerol, protein kinase C, and IκB-α
    Itani, SI
    Ruderman, NB
    Schmieder, F
    Boden, G
    [J]. DIABETES, 2002, 51 (07) : 2005 - 2011
  • [15] SUBSTRATE UTILIZATION AND ENZYMES IN SKELETAL-MUSCLE OF EXTREMELY ENDURANCE-TRAINED MEN
    JANSSON, E
    KAIJSER, L
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1987, 62 (03) : 999 - 1005
  • [16] SKELETAL-MUSCLE SUBSTRATE UTILIZATION DURING SUBMAXIMAL EXERCISE IN MAN - EFFECT OF ENDURANCE TRAINING
    KIENS, B
    ESSENGUSTAVSSON, B
    CHRISTENSEN, NJ
    SALTIN, B
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1993, 469 : 459 - 478
  • [17] INFLUENCE OF PHYSICAL-TRAINING ON THE FUEL-HORMONE RESPONSE TO PROLONGED LOW INTENSITY EXERCISE
    KOIVISTO, V
    HENDLER, R
    NADEL, E
    FELIG, P
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1982, 31 (02): : 192 - 197
  • [18] FATTY-ACID PATTERN OF LIPIDS IN NORMAL AND DYSTROPHIC HUMAN MUSCLE
    KUNZE, D
    REICHMANN, G
    EGGER, E
    OLTHOFF, D
    DOHLER, K
    [J]. EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1975, 5 (06) : 471 - 475
  • [19] LOWRY OH, 1951, J BIOL CHEM, V193, P265
  • [20] Lowry OH., 1972, FLEXIBLE SYSTEM ENZY